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对2025年根据欧盟委员会授权条例(EU)2018/772提交的监测报告进行年度评估。

Annual assessment of surveillance reports submitted in 2025 in the context of Commission Delegated Regulation (EU) 2018/772.

作者信息

Zancanaro Gabriele, Papaleo Stella

出版信息

EFSA J. 2025 Jul 24;23(7):e9526. doi: 10.2903/j.efsa.2025.9526. eCollection 2025 Jul.

Abstract

This report comprises the 15th assessment of the surveillance scientific reports, provided by Finland, Ireland, the United Kingdom (Northern Ireland) and Norway on their respective surveillance programmes. Every year since 2012, EFSA presents the assessment to the European Commission in which the sampling strategy, data collection and detection methods used by these countries are evaluated. More specifically, the surveillance programmes of these four countries are evaluated by checking the information submitted by each of them and verifying that the technical requirements were fulfilled as laid down in Commission Delegated Regulation (EU) 2018/772 of 21 November 2017 supplementing Regulation (EU) No 576/2013 of the European Parliament and of the Council with regard to preventive health measures for the control of infection in dogs, and repealing Delegated Regulation (EU) No 1152/2011. The information is divided into four different categories for assessment: the type and sensitivity of the detection method, the selection of the target population, the sampling strategy and the methodology. For each category, the main aspects that need to be considered to accomplish the technical requirements of the legislation are checked against compliance with several criteria. The countries participating in this surveillance (Finland, Ireland, the United Kingdom (Northern Ireland) and Norway) succeeded in the fulfilment of the technical legal requirements foreseen in Commission Delegated Regulation (EU) 2018/772 concerning these four different categories. None of the four countries recorded positive samples in the 12-month reporting period.

摘要

本报告包含芬兰、爱尔兰、英国(北爱尔兰)和挪威就各自监测计划提供的第15份监测科学报告评估。自2012年起,欧洲食品安全局(EFSA)每年都向欧盟委员会提交此项评估,其中对这些国家使用的抽样策略、数据收集和检测方法进行评估。更具体地说,通过检查这四个国家各自提交的信息,并核实其是否符合2017年11月21日欧盟委员会授权法规(EU)2018/772规定的技术要求,对这四个国家的监测计划进行评估。该法规补充了欧洲议会和理事会关于控制犬类感染的预防健康措施的(EU)No 576/2013号法规,并废止了(EU)No 1152/2011号授权法规。这些信息分为四类进行评估:检测方法的类型和灵敏度、目标人群的选择、抽样策略和方法。对于每一类,对照若干标准检查为满足立法技术要求需要考虑的主要方面是否合规。参与此项监测的国家(芬兰、爱尔兰、英国(北爱尔兰)和挪威)成功满足了欧盟委员会授权法规(EU)2018/772在这四类方面预见的技术法律要求。在12个月的报告期内,这四个国家均未检测到阳性样本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c32/12287657/c9b2fb0a3daf/EFS2-23-e9526-g007.jpg

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